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Letter to the Editor

Re: Daniel E. Spratt, Hebert A. Vargas, Zachary S.

Zumsteg, et al. Patterns of Lymph Node Failure after

Dose-escalated Radiotherapy: Implications for Extended

Pelvic Lymph Node Coverage. Eur Urol 2017;71:37–43

A Step Forward in the Era of Functional Imaging?

We read with interest the article by Spratt and colleagues

[1]

recently published in

European Urology

. The authors

analyzed patterns of abdominopelvic lymph node (LN)

failure via radiographic LN mapping in a large series of

prostate cancer (PC) patients treated with definitive dose-

escalated radiation therapy (RT) without pelvic LN RT.

In their experience, radiographic failures were most

frequently found above the L5/S1 landmark. Thus, for

selected PC patients, the current pelvic LN RT recommen-

dation could be revisited. The authors state that androgen

deprivation therapy could prevent or minimize marginal

and/or out-of-field recurrences. Moreover, Spratt et al

[1]

recommended revisiting of the current RT field recommen-

dation for pelvic LNs (up to the superior border of the

internal/external iliac vessels) because of inadequate RT

coverage.

Looking at their findings

[1] ,

a type of pelvic RT volume

customization could be introduced in clinical practice. In

fact, in the analysis by Spratt et al

[1]

, PC patients with

Gleason score 8 were at particular risk of dissemination to

distant nodes. However, this PC category deserves accurate

pre-RT staging to exclude distant dissemination

[2]

. Recent

data support the value of molecular imaging in the

therapeutic approach to high-risk PC. The reliability of

new tracers (such as

11

C- and

18

F-choline and/or

68

Ga-

labeled prostate-specific membrane antigen [PSMA]) for PC

has been investigated in several series

[3] .

While choline

positron emission tomography (PET) is not indicated for

routine local tumor staging, it seems to have better

performance than conventional morphological imaging in

LN staging and for all PC patients with suspected distant

metastases. In addition,

68

Ga-PSMA seems to be more

sensitive and specific than choline

[4]

. All these molecular

imaging advances should be introduced to pre-RT target

assessment procedures to modify the treatment strategy in

terms of: (1) changes in treatment intent from radical to

palliative; (2) changes in RT volumes and doses; and (3)

integration with other therapies

[3]

. Unfortunately, Spratt

et al

[1]

only included PC patients with complete abdominal

and pelvic imaging with magnetic resonance imaging,

computed tomography (CT), and/or fluorodeoxyglucose

PET/CT to determine the pattern of nodal relapses, and

more specific and sensitive staging tools (eg, choline PET

and/or PSMA PET) were not used. Undoubtedly, this

methodology could affect the real value of the results,

and probably resulted in underestimation of the real PC

staging.

An ongoing trial, RTOG 0924, as mentioned by the

authors

[1]

, will evaluate the impact of extended pelvic RT

in selected PC patients. From our point of view, in the

absence of accurate pre-RT staging with functional imaging,

the issue of pelvic node RT will remain controversial.

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

Spratt DE, Vargas HA, Zumsteg ZS, et al. Patterns of lymph node failure after dose-escalated radiotherapy: implications for extend- ed pelvic lymph node coverage. Eur Urol 2017;71:37–43.

[2]

Alongi F, Fersino S, Giaj Levra N, et al. Impact of 18 F-choline PET/CT in the decision-making strategy of treatment volumes in definitive prostate cancer volumetric modulated radiation therapy. Clin Nucl Med 2015;40:e496–500

.

[3]

De Bari B, Alongi F, Lestrade L, Giammarile F. Choline-PET in prostate cancer management: the point of view of the radiation oncologist. Crit Rev Oncol Hematol 2014;91:234–47

.

[4]

Afshar-Oromieh A, Haberkorn U, Schlemmer HP, et al. Comparison of PET/CT and PET/MRI hybrid systems using a 68 Ga-labelled PSMA ligand for the diagnosis of recurrent prostate cancer: initial experi- ence. Eur J Nucl Med Mol Imaging 2014;41:887–97

.

E U R O P E A N U R O L O G Y 7 1 ( 2 0 1 7 ) e 1 2 1 – e 1 2 2

ava ilable at

www.sciencedirect.com

journal homepage:

www.eu ropeanurology.com

DOI of original article:

http://dx.doi.org/10.1016/j.eururo.2016.07.043

.

http://dx.doi.org/10.1016/j.eururo.2016.10.050

0302-2838/

#

2016 European Association of Urology. Published by Elsevier B.V. All rights reserved.